Berberine and Non-Alcoholic Fatty Liver Disease (NAFLD)

A seven-week (45-day), open-label, randomized controlled trial was conducted in a medical center affiliated with the Ministry of Welfare and Social Security in Iran to study the impact of berberine on liver function and metabolic profiles of patients with NAFLD. Hospital employees who met the enrollment criteria were identified through electronic health records (EHRs) available in a human resource database of employee routine annual examinations. Using a computer-generated random-allocation sequence, eligible employees were equally assigned (1:1) to berberine 6.25 g per day (arm A) or no intervention (Arm B). Berberine was administered orally (100 g dried berberine in 5 Liter water boiled at 167°F until 4Liter).). To control the potential impact of confounders on outcome measures, and to balance the daily dietary and physical activity among the study groups, all participants were trained by skilled experts on lifestyle and behavior improvement.

Inclusion criteria

• Patients must have an age range between 18 to 65 years(inclusive).
• Patients with Liver fat content assessed by MRS≥13%.
• Patients must meet the criteria for impaired glucose regulation
• Course of diabetic mellitus less than 1 year
• Informed consent signed

Exclusion criteria

• Any causes of chronic liver disease other than NAFLD(such as-but not restricted to- alcohol or drug abuse, medication, chronic hepatitis B or C, autoimmune, etc.);

• Patients with significantly impaired liver function: ALT or AST≥2 times upper limit of normal;
• Patients with type 1 diabetes mellitus or gestational diabetes or special type diabetes;
• Course of diabetes more than 1 years;
• Diabetics patients who have taken or are taking oral glucose-lowering drugs or insulin;
• Diabetics patients with a HbA1c>7.5% on initial visit;
• Patients with severe diabetes complications(diabetes ketoacidosis, diabetes coma or with symptomatic of diabetes coma; dysfunction of nerve, retinopathy, dysfunction of kidney);
• Patients with a history of clinically significant heart disease(myocardial infarct, heart failure, and/or severe cardiac rhythm);
• Complicating severe infection,within 6 months after operation, severe trauma;
• Patients with excess alcohol consumption≥140g/week(male); ≥70g/week(female);
• Patients have participated other clinical trials within 24 weeks;
• Patients with a history of drug allergy to berberine;
• Patients with gestation or possible gestation or lactation, or males or females expecting gestation during clinical trial;
• Mental diseases patients;
• Those who refuse to sign informed consent;
• Any other conditions, which, in the opinion of the investigators would impede competence or compliance or possibility of hindering completion of the study;
• Patients with serum triglyceride≥5.0mmol/L;
• Patients with thyroid disease, including hyperthyroidism or hypothyroidism.